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The Supply Chain Planner/Scheduler is responsible for demand planning, inventory management, and ensuring quality and timely delivery of products. The role involves creating detailed plans and schedules, overseeing purchasing cycles, and providing direction to manufacturing teams.

The Quality Systems Lead will enhance the Quality Management System (QMS), focusing on electronic support, risk assessments, inspection readiness, and compliance. Responsibilities include managing the QMS platform, facilitating training, conducting audits, and supporting continuous improvement initiatives. The role demands a proactive individual to ensure regulatory compliance and improve quality systems across the organization.

The Automation Engineer II handles the administration of facilities and process automation, providing support and troubleshooting services. Responsibilities include designing and implementing automation systems, leading projects for equipment modifications, and developing test scripts and automation procedures.

The QC Analyst I is responsible for routine and non-routine QC testing per SOPs, conducting analytical testing and managing quality systems including deviations and CAPAs in compliance with cGMP guidelines.

The Process Engineer will manage engineering projects for gene therapy processes, focusing on workflow optimization, compliance with FDA and EU standards, and continuous improvements. Responsibilities include project management, quality control, and ensuring adherence to safety and environmental protocols while driving operational efficiency.

The role involves directing the development of upstream processes for viral vector production, optimizing processes for robustness and yield, and ensuring compliance with GMP standards. Responsibilities include experiment design, monitoring performance, and maintaining relationships with stakeholders and suppliers.

The Quality Operations Associate will oversee quality assurance processes within manufacturing and quality control areas, ensuring compliance with regulations and internal policies. Responsibilities include quality oversight during operations, SOP development, documentation accuracy review, and providing training on GMP and GDP. The role also involves conducting root cause analysis of quality events and collaborating with various departments for quality assurance.